SLC25A1 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC25A1
Gene name solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
Chromosome 22
Chromosomal band q11
Imprinted Unknown
Genomic reference NC_000022.10
Transcript reference NM_001256534.1, NM_005984.3, NR_033687.2, NR_046298.1
Associated with diseases D2L2AD
Citation reference(s) -
Curators (0) -
Total number of public variants reported 12
Unique public DNA variants reported 6
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Notes MSeqDR-LSDB
Date created November 15, 2013
Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer
Links to other resources
HGNC 10979
Entrez Gene 6576
PubMed articles SLC25A1
OMIM - Gene 190315
OMIM - Diseases D2L2AD (Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3))
HGMD SLC25A1
GeneCards SLC25A1
GeneTests SLC25A1


Active transcripts


ID     
Chr     
Name     
NCBI ID     
NCBI Protein ID     
DescendingVariants     
00002843 22 transcript variant 4 NR_046298.1 - 12
00002844 22 transcript variant 1 NM_005984.3 NP_005975.1 12
00002845 22 transcript variant 2 NR_033687.2 - 12
00002846 22 transcript variant 3 NM_001256534.1 NP_001243463.1 12


Copyright & disclaimer
; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

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